Canonical Allele Identifier: CA1427019587

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620652G= , CM000665.2:g.186620652G=	GRCh38
NC_000003.11:g.186338441G= , CM000665.1:g.186338441G=	GRCh37
NC_000003.10:g.187821135G=	NCBI36
NG_011436.1:g.12592G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.826G= MANE Select	ENSP00000393887.2:p.Asp276=
ENST00000273784.5:c.829G=	ENSP00000273784.5:p.Asp277=
ENST00000411641.6:c.826G=	ENSP00000393887.2:p.Asp276=
NM_001622.2:c.826G=	NP_001613.2:p.Asp276=
NM_001354571.1:c.829G=	NP_001341500.1:p.Asp277=
NM_001354572.1:c.823G=	NP_001341501.1:p.Asp275=
NM_001354573.1:c.742G=	NP_001341502.1:p.Asp248=
NM_001622.3:c.826G=	NP_001613.2:p.Asp276=
NM_001622.4:c.826G= MANE Select	NP_001613.2:p.Asp276=
NM_001354571.2:c.829G=	NP_001341500.1:p.Asp277=
NM_001354572.2:c.823G=	NP_001341501.1:p.Asp275=
NM_001354573.2:c.742G=	NP_001341502.1:p.Asp248=